Combination therapy for treatment of cancer
A technology of cancer, therapeutic agent, applied in the field of combination therapy for the treatment of cancer, capable of solving problems such as undifferentiated, uncontrolled proliferation
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Embodiment 1
[0298] Activity of FZD8-Fc Soluble Receptor OMP-54F28 in Combination with Chemotherapeutic Agents in Vivo
[0299] The OncoMed xenograft models described herein were established at OncoMed Pharmaceuticals from minimally passaged patient-derived tumor specimens. Tumor samples are examined by a pathologist and classified into specific tumor types. OncoMed relies on these classifications unless further analysis is performed on any particular tumor and reclassification is deemed warranted.
[0300] Xenograft OMP-OV19 ovarian tumor cells (1×10 5 cells) were injected subcutaneously into 6-8 week-old NOD / SCID mice. Tumors were grown for 28 days until they reached 120mm 3 average volume. Mice were randomly divided into groups (n=9 per group) and treated with paclitaxel, nab-paclitaxel, carboplatin, combination of carboplatin and paclitaxel, combination of OMP-54F28 and paclitaxel, combination of OMP-54F28 and nab-paclitaxel Mice were treated with the combination, the combination ...
Embodiment 2
[0305] Effect of Staggered Dosing Regimen on the Activity of Anti-FZD Antibody OMP-18R5 in Combination with Paclitaxel
[0306] Single cell suspensions of xenografted UM-PE13 mammary tumor cells (20,000 cells) were injected subcutaneously into 6-8 week old NOD / SCID mice. UM-PE13 is a type of triple negative breast cancer. Tumors were allowed to grow for 34 days until they reached an average of 80mm 3 volume of. Mice were randomly divided into groups (n=8 per group) and treated with paclitaxel, a combination of OMP-18R5 and paclitaxel administered on the same day, a combination of OMP-18R5 and paclitaxel (where paclitaxel was administered 3 days before the administration of OMP-18R5), A combination of OMP-18R5 and paclitaxel (wherein OMP-18R5 was administered 3 days prior to paclitaxel administration), or a control antibody treated mice. Mice were treated every three weeks with OMP-18R5 at a dose of 25 mg / kg and paclitaxel at a dose of 20 mg / kg. OMP-18R5 and paclitaxel were...
Embodiment 3
[0310] Effect of Staggered Dosing Regimen on the Activity of FZD8-Fc Soluble Receptor OMP-54F28 in Combination with Paclitaxel
[0311] Xenograft OMP-OV38 ovarian tumor cells (1×10 5 cells) were injected subcutaneously into 6-8 week-old NOD / SCID mice. Tumors were grown for 38 days until they reached 140mm 3 average volume. Mice were randomly divided into groups (n=9 per group) and treated with paclitaxel, a combination of OMP-54F28 and paclitaxel administered on the same day, a combination of OMP-54F28 and paclitaxel (where paclitaxel was administered 2 days before the administration of OMP-54F28), OMP Mice were treated with a combination of 54F28 and paclitaxel (where OMP-54F28 was administered 2 days prior to paclitaxel administration) or a control antibody. Mice were treated biweekly with OMP-54F28 at a dose of 25 mg / kg and paclitaxel at a dose of 20 mg / kg. OMP-54F28 and paclitaxel were administered intraperitoneally. Tumor growth was monitored and tumor volume was mea...
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